陶瓷法制备Ni0.7Zn0.3Fe2O4+0.6wt%V2O5的x射线衍射、红外光谱和磁性能

M. S. Patil
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引用次数: 0

摘要

鉴于对添加剂的需求日益增长,我们采用陶瓷技术促进了负载0.6wt%V2O5的Ni0.7Zn0.3Fe2O4的复合形成。结构分析和磁性是通过不同的表征技术来确定的。用XRD谱分析了添加V2O5后的相形成和纯度。在红外光谱中,通过定位Ni0.7Zn0.3Fe2O4+0.6wt%V2O5的本征振动带,对Ni0.7Zn0.3Fe2O4+0.6wt%V2O5的官能团进行了检查,并确定了相的形成。通过对XRD数据的事后检验,计算了晶格常数(a)和x射线密度(dx)。我们注意到Ni0.7Zn0.3Fe2O4+0.6wt%V2O5的饱和磁化强度(Ms)、剩磁磁化强度(Mr)和磁子数(nB)的膨胀是V2O5加载的主要原因。承认,矫顽力率(Hc)急剧下降,表明交替磁参数。研究了添加0.6wt%V2O5对Ni0.7Zn0.3Fe2O4铁氧体物理性能的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
X-ray diffraction, infra-red spectroscopy and magnetic properties of Ni0.7Zn0.3Fe2O4+0.6wt%V2O5 prepared via ceramic method
In view of the growing demand to the additives, we promote the compound formation of Ni0.7Zn0.3Fe2O4 loaded with 0.6wt%V2O5 by ceramic technique. The structural analysis and magnetic were determined by diverse characterization techniques. The phase formation and purity over the addition of V2O5 was identified by XRD pattern. In IR studied, the functional group scrutiny of Ni0.7Zn0.3Fe2O4+0.6wt%V2O5 was examined by locating the intrinsic vibrational bands and confirmed the phase formation. The lattice constant (a) and x-ray density (dx) were calculated from the post-examination of XRD data. We noted an inflation in the Saturation magnetization (Ms), Remanence magnetization (Mr) and magneton number (nB) of Ni0.7Zn0.3Fe2O4+0.6wt%V2O5 as a principle cause of V2O5 loading. Admitting that, the rate of coercivity (Hc) was drastically declined suggesting the alternated magnetic parameters. This inspection was focused on the characteristic ramification of additive 0.6wt%V2O5 on physical properties of Ni0.7Zn0.3Fe2O4 ferrite.
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